1999 organo-phosphorus compounds, acyclic C derivatives organo-phosphorus compounds, acyclic C derivatives S 0082 27 - 186 The Preparation of (EtO) 2 P(O)CFHZnBr and (EtO) 2 P(O)CFHCu and Their Utility in the Preparation of Functionalized α- Fluorophosphonates. — The organic reagent (I) or the corresponding Cu(I)-compound, generated in situ by transmetalation with CuBr, react readily with a variety of organic halides to yield functionalized α-ﬂuorophosphonates directly. — (ZHANG, XIN; QIU, WEIMING; BURTON, DONALD J.; Tetrahedron Lett. 40 (1999) 14, 2681-2684; Dep. Chem., Univ. Iowa, Iowa City, IA 52242, USA; EN) 1

ChemInform Abstract: The Preparation of (EtO)2P(O)CFHZnBr and (EtO)2P(O)CFHCu and Their Utility in the Preparation of Functionalized α-Fluorophosphonates

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Page 1: ChemInform Abstract: The Preparation of (EtO)2P(O)CFHZnBr and (EtO)2P(O)CFHCu and Their Utility in the Preparation of Functionalized α-Fluorophosphonates

1999 organo-phosphorus compounds, acyclic C derivatives

organo-phosphorus compounds, acyclic C derivativesS 0082

27 - 186The Preparation of (EtO)2P(O)CFHZnBr and (EtO)2P(O)CFHCuand Their Utility in the Preparation of Functionalized α-Fluorophosphonates. — The organic reagent (I) or the correspondingCu(I)-compound, generated in situ by transmetalation with CuBr, react readilywith a variety of organic halides to yield functionalized α-fluorophosphonatesdirectly. — (ZHANG, XIN; QIU, WEIMING; BURTON, DONALD J.;Tetrahedron Lett. 40 (1999) 14, 2681-2684; Dep. Chem., Univ. Iowa, Iowa City,IA 52242, USA; EN)